Hemoglobinopathies Among Patients Referred to Single Centre in Central India: An Observational Study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s12291-023-01151-2.pdf
Reference25 articles.
1. Williams TN, Weatherall DJ. World distribution, population genetics, and health burden of the hemoglobinopathies. Cold Spring Harb Perspect Med. 2012;2(9):a011692. https://doi.org/10.1101/cshperspect.a011692.
2. WHO. Management of hemoglobin disorders: Report of a Joint WHO-TIF meeting. https://www.who.int/genomics/WHO-TIF_genetics_final.pdf?ua=1. Accessed 14 April 2023
3. Colah RB, Mukherjee MB, Martin S, Ghosh K. Sickle cell disease in tribal populations in India. Indian J Med Res. 2015;141(5):509–15. https://doi.org/10.4103/0971-5916.159492.
4. Hockham C, Bhatt S, Colah R, Mukherjee MB, Penman BS, Gupta S, et al. The spatial epidemiology of sickle-cell anaemia in India. Sci Rep. 2018;8(1):17685. https://doi.org/10.1038/s41598-018-36077-w.
5. Mohanty D, Colah RB, Gorakshakar AC, Patel RZ, Master DC, Mahanta J, et al. Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study. J Commun Genet. 2013;4(1):33–42. https://doi.org/10.1007/s12687-012-0114-0.
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